Kesatuan Eropah - Poland - EMA (European Medicines Agency)

pfizer europe ma eeig  - abrocitinib - zapalenie skóry, atopowe - inne preparaty dermatologiczne - cibinqo is indicated for the treatment of moderate-to-severe atopic dermatitis in adults who are candidates for systemic therapy.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

pfizer europe ma eeig - somatrogon - growth and development - przysadka i podwzgÓrze hormony i odpowiedniki - indicated for the long-term treatment of paediatric patients with growth disturbance due to insufficient secretion of growth hormone.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 8, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 10a, pneumococcal polysaccharide serotype 11a, pneumococcal polysaccharide serotype 12f, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 15b, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 22f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 33f - infekcje pneumokokowe - szczepionki - active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. zobacz rozdziały 4. 4 i 5. 1 w celu uzyskania informacji na temat ochrony przed określonymi serotypami pneumokokowymi. apexxnar should be used in accordance with official recommendations. .

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

pfizer europe ma eeig - respiratory syncytial virus, subgroup a, stabilized prefusion f protein / respiratory syncytial virus, subgroup b, stabilized prefusion f protein - infekcje wirusem oddechowym - szczepionki - abrysvo is indicated for:passive protection against lower respiratory tract disease caused by respiratory syncytial virus (rsv) in infants from birth through 6 months of age following maternal immunisation during pregnancy. zobacz rozdziały 4. 2 i 5. active immunisation of individuals 60 years of age and older for the prevention of lower respiratory tract disease caused by rsv. stosowanie tej szczepionki powinno odbywać się zgodnie z oficjalnymi zaleceniami.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

pfizer europe ma eeig - wareniklina - zaprzestanie palenia tytoniu - inne leki na układ nerwowy - champix jest wskazany do rzucania palenia u dorosłych.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

pfizer europe ma eeig - kryzotynib - rak, niedrobnokomórkowe płuca - Środki przeciwnowotworowe - xalkori as monotherapy is indicated for:the first‑line treatment of adults with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with previously treated anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with ros1‑positive advanced non‑small cell lung cancer (nsclc)the treatment of paediatric patients (age ≥6 to.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

pfizer europe ma eeig - worykonazol - candidiasis; mycoses; aspergillosis - Środki przeciwgrzybicze do stosowania ogólnego - worykonazolu, o szerokim spektrum, триазольное środek przeciwgrzybiczny i jest wskazany u dorosłych i dzieci w wieku od 2 lat i powyżej w następujący sposób:leczenie aspergilozy inwazyjnej;leczenie w candidaemianon-pacjentów z neutropenią;leczenie flukonazol-odporne na poważne inwazyjne zakażenia candidal (w tym z. krusei);leczenie poważne infekcje grzybicze zakażenia, spowodowane przez scedosporium spp i. i fusarium ѕрр. vfend należy wyznaczyć w pierwszej kolejności u pacjentów z postępującą, być może, zagrażających życiu zakażeń. profilaktyka inwazyjnych zakażeń grzybiczych w grupie wysokiego ryzyka allogenicznego przeszczepienia krwiotwórczych komórek macierzystych (ТГСК) odbiorców.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

pfizer europe ma eeig - Тофацитиниб - zapalenie stawów, reumatoidalne - leki immunosupresyjne - rheumatoid arthritistofacitinib in combination with methotrexate (mtx) is indicated for the treatment of moderate to severe active rheumatoid arthritis (ra) in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying antirheumatic drugs (dmards) (see section 5. tofacitinib can be given as monotherapy in case of intolerance to mtx or when treatment with mtx is inappropriate (see sections 4. 4 i 4. psoriatic arthritistofacitinib in combination with mtx is indicated for the treatment of active psoriatic arthritis (psa) in adult patients who have had an inadequate response or who have been intolerant to a prior disease modifying antirheumatic drug (dmard) therapy (see section 5. ulcerative colitistofacitinib is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent (see section 5. tofacitinib is indicated for the treatment of active polyarticular juvenile idiopathic arthritis (rheumatoid factor positive [rf+] or negative [rf-] polyarthritis and extended oligoarthritis), and juvenile psoriatic arthritis (psa) in patients 2 years of age and older, who have responded inadequately to previous therapy with disease modifying antirheumatic drugs (dmards). tofacitinib can be given in combination with methotrexate (mtx) or as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. ankylosing spondylitistofacitinib is indicated for the treatment of adult patients with active ankylosing spondylitis (as) who have responded inadequately to conventional therapy.

Poland - Poland - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

pfizer europe ma eeig - doxorubicini hydrochloridum - proszek i rozpuszczalnik do sporządzania roztworu do wstrzykiwań - 10 mg

Poland - Poland - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

pfizer europe ma eeig - doxorubicini hydrochloridum - proszek do sporządzania roztworu do wstrzykiwań - 50 mg